Enediynes via sequential acetylide reductive coupling and alkyne metathesis: Easy access to well-defined molybdenum initiators for alkyne metathesis

被引:57
作者
Blackwell, JM [1 ]
Figueroa, JS [1 ]
Stephens, FH [1 ]
Cummins, CC [1 ]
机构
[1] MIT, Cambridge, MA 02139 USA
关键词
D O I
10.1021/om0301482
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A new synthetic route utilizes the reductive coupling of molybdenum(IV) acetylides toward the construction of both enediyne molecules and trialkoxymolybdenum alkylidynes, the latter being useful as alkyne metathesis initiators. The molybdaziridine hydride complex Mo(H)(eta(2)-Me2CNAr)(N[i-Pr]Ar)(2), 1, readily prepared from MoCl3(thf)(3), is elaborated in three generally high-yielding steps to enediynes and/or metathesis catalysts.
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页码:3351 / 3353
页数:3
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